...
首页> 外文期刊>Electrochimica Acta >Properties of sol-gel SnO{sub}2/TiO{sub}2 electrodes and their photoelectrocatalytic activities under UV and visible light illumination
【24h】

Properties of sol-gel SnO{sub}2/TiO{sub}2 electrodes and their photoelectrocatalytic activities under UV and visible light illumination

机译:溶胶-凝胶SnO {sub} 2 / TiO {sub} 2电极的性能及其在紫外和可见光照射下的光电催化活性

获取原文
获取原文并翻译 | 示例

摘要

A visible light active binary SnO{sub}2-TiO{sub}2 composite was successfully prepared by a sol-gel method and deposited on Ti sheet as a photoanode to degrade orange II dye. Titanium and SnO{sub}2 can promote the development of rutile phase of TiO{sub}2 and inhibit the formation of anatase phase of TiO{sub}2. Formation of SnO{sub}2 crystalline is insignificant even when the calcination temperature increases to 700℃. Heterogenized interface between SnO{sub}2 and TiO{sub}2 inhibits growth of TiO{sub}2 linkage and leads to the particle-filled surface morphology of SnO{sub}2-containing films. The carbonaceous, Ti-O-C bonds and Ti{sup}(3+) species are likely to account for the photoabsorption and photoelectrocatalytic (PEC) activity under visible light illumination. The electrode with 30% SnO{sub}2 exhibits higher photocurrent when compared with those in the region of 0-50%. The 600℃-calcined SnO{sub}2-TiO{sub}2 electrode indicates higher activity when compared with those at 400, 500, 700 and 800℃. PEC degradation of orange II follows the Langmuir-Hinshelwood model and takes place much effectively in a solution of pH 3.0 than those in pH 7.0 and pH 11.0.
机译:通过溶胶-凝胶法成功制备了可见光活性的二元SnO {sub} 2-TiO {sub} 2复合材料,并沉积在Ti板上作为光阳极降解橙色II染料。钛和SnO {sub} 2可以促进TiO {sub} 2的金红石相的发展,并抑制TiO {sub} 2的锐钛矿相的形成。即使煅烧温度升至700℃,SnO {sub} 2晶体的形成也微不足道。 SnO {sub} 2和TiO {sub} 2之间的异质界面抑制TiO {sub} 2键的生长,并导致含SnO {sub} 2的薄膜充满颗粒的表面形态。碳质,Ti-O-C键和Ti {sup}(3+)物种可能解释了在可见光照射下的光吸收和光电催化(PEC)活性。与0-50%范围内的电极相比,具有30%SnO {sub} 2的电极表现出更高的光电流。 600℃煅烧的SnO {sub} 2-TiO {sub} 2电极与400、500、700和800℃相比具有更高的活性。橙色II的PEC降解遵循Langmuir-Hinshelwood模型,并且在pH 3.0的溶液中比在pH 7.0和pH 11.0的溶液中更有效地发生。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号